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Clinical Trials/TCTR20221011002
TCTR20221011002
Completed
Phase 4

Acetaminophen and Chlorpheniramine Maleate Premedication in Chronically Transfused Patients: A Prospective, Randomized Controlled Trial

Supanat Janyangam0 sites94 target enrollmentOctober 11, 2022

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Efficacy of chlorpheniramine maleate and acetaminophen premedication in prevent febrile nonhemolytic transfusion reaction in chronically transfused patient.
Sponsor
Supanat Janyangam
Enrollment
94
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 11, 2022
End Date
January 4, 2023
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Supanat Janyangam

Eligibility Criteria

Inclusion Criteria

  • 1\. Patient receiving red cell transfusion at least 2 unit from the same cause in the last 3 months
  • 2\. Hemoglobin level before transfusion is below 8 gm/dL
  • 3\. At least 18 years of age

Exclusion Criteria

  • 1\. Patient receiving red cell transfusion from acute blood loss
  • 2\. Patient receiving red cell transfusion related to trauma
  • 3\. Patient receiving red cell transfusion related to surgery
  • 4\. History of febrile illness following transfusion in the last 3 months
  • 5\. History of allergic reaction following transfusion in the last 3 months
  • 6\. Acetaminophen allergy
  • 7\. Chlorpheniramine maleate allergy
  • 8\. Febrile illness within 24 hours prior to transfusion
  • 9\. Allergic reaction within 24 hours prior to transfusion
  • 10\. Patient receiving acetaminophen, chlorpheniramine maleate, other antihistamine, or corticosteroid equivalent to 5mg of prednisolone within 48 hours prior to transfusion

Outcomes

Primary Outcomes

Not specified

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